Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9423417-9423720 | Rare:98 | ||||
chr2:9474505-9474640 | Common:6; Rare:67 | ||||
chr2:9843250-9843521 | Common:6; Rare:79 | ||||
chr2:10043418-10043568 | Common:3; Rare:66 | ||||
chr2:10122573-10122785 | Common:4; Rare:97 | ||||
chr2:10302772-10302991 | Common:4; Rare:59 | ||||
chr2:10448321-10448671 | Common:1; Rare:102 | ||||
chr2:10689940-10690023 | Common:1; Rare:25 | ||||
chr2:10812697-10813063 | Common:5; Rare:140 | ||||
chr2:12716742-12717056 | Common:1; Rare:89 | ||||
chr2:17753731-17754189 | Common:5; Rare:145; Clinvar (benign):1 | ||||
chr2:19901664-19901759 | Common:1; Rare:48 | ||||
chr2:20051550-20051826 | Common:1; Rare:73 | ||||
chr2:23940379-23940635 | Common:4; Rare:82 | ||||
chr2:24076206-24076561 | Rare:96 |